Canonical Allele Identifier: CA352199981

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39390506C>G , CM000665.2:g.39390506C>G	GRCh38
NC_000003.11:g.39431997C>G , CM000665.1:g.39431997C>G	GRCh37
NC_000003.10:g.39407001C>G	NCBI36
NG_016931.1:g.12183C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_017875.4:c.275C>G MANE Select	NP_060345.2:p.Pro92Arg
ENST00000650617.1:c.275C>G MANE Select	ENSP00000497532.1:p.Pro92Arg
NM_001354798.1:c.275C>G	NP_001341727.1:p.Pro92Arg
NM_001354798.2:c.275C>G	NP_001341727.1:p.Pro92Arg
NM_017875.2:c.275C>G	NP_060345.2:p.Pro92Arg
ENST00000273158.8:c.275C>G	ENSP00000273158.3:p.Pro92Arg
ENST00000431510.1:c.263C>G	ENSP00000394244.1:p.Pro88Arg
ENST00000642442.1:n.336C>G
ENST00000642683.1:c.228+47C>G	ENSP00000495376.1:n.228+47C>G
ENST00000642978.1:c.257C>G	ENSP00000494342.1:p.Pro86Arg
ENST00000643672.1:c.224C>G	ENSP00000494532.1:p.Pro75Arg
ENST00000645280.1:c.221C>G	ENSP00000496690.1:p.Pro74Arg
ENST00000645630.1:c.275C>G	ENSP00000493714.1:p.Pro92Arg
ENST00000648579.1:c.275C>G	ENSP00000497638.1:p.Pro92Arg
XM_006713214.1:c.263C>G	XP_006713277.1:p.Pro88Arg
XM_006713214.2:c.263C>G	XP_006713277.1:p.Pro88Arg
XM_011533869.1:c.257C>G	XP_011532171.1:p.Pro86Arg
XM_011533869.2:c.257C>G	XP_011532171.1:p.Pro86Arg
XM_011533870.1:c.224C>G	XP_011532172.1:p.Pro75Arg
XM_011533871.1:c.275C>G	XP_011532173.1:p.Pro92Arg
XM_024453611.1:c.221C>G	XP_024309379.1:p.Pro74Arg